Pill Identifier Bupropion Hydrochloride - NDC 47335-954
Bupropion Hydrochloride
Product Code 47335-954
Bupropion Hydrochloride by Sun Pharmaceutical Industries, Inc. is a orange and white rou tablet extended release about 8 mm in size, imprinted with 954. The product is a human prescription drug with active ingredient(s) bupropion hydrochloride.
Bupropion Hydrochloride
Active Ingredient(s): Bupropion Hydrochloride
Inactive Ingredient(s):
- HYDROXYPROPYL CELLULOSE (1600000 WAMW)
- SACCHARIN
- LACTOSE MONOHYDRATE
- SILICON DIOXIDE
- TALC
- STEARIC ACID
- CELLULOSE, MICROCRYSTALLINE
- CROSPOVIDONE
- FD&C YELLOW NO. 6
- POLYVINYL ALCOHOL
- POLYETHYLENE GLYCOL, UNSPECIFIED
- POLYSORBATE 80
- ETHYLCELLULOSES
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- TRIETHYL CITRATE
- SODIUM BICARBONATE
- SODIUM LAURYL SULFATE
- DIBUTYL SEBACATE
- SHELLAC
- FERROSOFERRIC OXIDE
- BUTYL ALCOHOL
- PROPYLENE GLYCOL
- ISOPROPYL ALCOHOL
- AMMONIA
Sun Pharmaceutical Industries, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Extended Release
- Orange (C48331)
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
47335-954-13 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE |
47335-954-81 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE |
47335-954-83 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE |
* Please review the disclaimer below.
Pill Identification data last updated on: December, 2018
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product. If this is an emergency, call 911 or the national Poison Help hotline at 1-800-222-1222. Most images are not part of the product labels and have not been verified by the labeler company. ALWAYS consult your physician or pharmacist with any medication-related questions.